ATHEROSCLEROTIC NEPHROPATHY. CLINIC ASPECTS OF POLYCYSTIC KIDNEY DISEASE

Khasanova M.A., Umarova Z.F.

Ёш олимлар тиббиёт журнали · 2024-yil

Annotatsiya

Cystic kidneys are common causes of end–stage renal disease, both in children and in adults. Autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD) are cilia–related disorders and the two main forms of monogenic cystic kidney diseases. ADPKD is a common disease that mostly presents in adults, whereas ARPKD is a rarer and often more severe form of polycystic kidney disease (PKD) that usually presents perinatally or in early childhood. We review the pathophysiologic patterns and recent advances in the clinical pharmacotherapy of autosomal dominant PKD. A multipronged approach with pharmacologic and nonpharmacologic treatments can be successfully used to slow down the rate of progression of autosomal dominant PKD to kidney failure.

Maqola ma’lumotlari
MualliflarKhasanova M.A., Umarova Z.F.
JurnalЁш олимлар тиббиёт журнали
Nashr sanasi2024-12-09
Son12
Betlar195-202
TilRus

Kalit so‘zlar

Polycystic kidney disease, chronic kidney disease, autosomal dominant polycystic kidney disease.

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